Senior Clinical Research Associate

JR United Kingdom; Chesterfield; Remote; GBP 50,000 - 56,000; Full time

Job summary

A leading life sciences consulting firm is seeking a Senior Clinical Research Associate to manage investigator sites for clinical studies. This role entails conducting monitoring visits and ensuring compliance with relevant regulations. Ideal candidates will have a BSc in a health-related field and significant CRA experience, supporting innovative healthcare solutions.

Qualifications

• Minimum of 3 years proven CRA experience.
• Broad knowledge of medical terminology and clinical patient management.
• Basic understanding of drug therapy techniques.

Responsibilities

• Manage investigator sites independently throughout the study lifecycle.
• Conduct feasibility and monitoring visits for research sites.
• Report and follow-up on adverse and serious adverse events.

Skills

Knowledge of medical terminology

Patient management

Clinical research methodologies

Education

BSc in a health-related field

Job description

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Senior Clinical Research Associate, Chesterfield

Client: RBW Consulting

Location: Chesterfield, United Kingdom

Job Category: Other

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EU work permit required:

Yes

Job Views:

4

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

• Job Title: Senior Clinical Research Associate
• Location: Remote in UK
• Salary: £50,000 - £56,000 plus car allowance or company car
• Company: Global CRO

RBW Consulting is excited to present an opportunity on behalf of a renowned CRO focused on healthcare intelligence and European culture. The company specializes in addressing unmet disease targets and advancing clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Key accountabilities

• Manage investigator sites independently throughout the study lifecycle (start-up to close-out);
• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3, across all therapeutic areas;
• Prepare for and attend investigator meetings, ensuring timely delivery, proper storage, and accountability of clinical supplies, and follow-up on drug safety issues;
• Verify source documents and review case report forms;
• Review regulatory documents;
• Report and follow-up on adverse and serious adverse events;
• Assess patient recruitment and retention.

Qualifications

• BSc in a health-related field or equivalent;
• Minimum of 3 years proven CRA experience;
• Broad knowledge of medical terminology and clinical patient management;
• Basic understanding of drug therapy techniques and clinical research methodologies.

To apply:

Please click ‘apply’ or contact Joe Pearce for further information.

About RBW Consulting

RBW Consulting is a life sciences talent and strategic consultancy committed to supporting innovation in healthcare. We help life sciences companies deliver better health outcomes by providing the right people, insights, and networks. We foster a culture of support, transparency, and mutual commitment, prioritizing people over short-term gains.

Equal Opportunity Statement

RBW Consulting is an equal opportunity employer. We value diversity and do not discriminate based on race, ethnicity, color, sex, gender identity or expression, sexual orientation, religion, age, marital status, disability, medical condition, national origin, veteran status, or any other protected characteristic. We are dedicated to building a diverse workforce that reflects various backgrounds, perspectives, and skills.